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SEASIGHT ESR Test Pipette (3.8% Sodium Citrate) - Indonesia BPOM Medical Device Registration

SEASIGHT ESR Test Pipette (3.8% Sodium Citrate) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20206420018. The device is manufactured by ZHEJIANG SORFA LIFE SCIENCE RESEARCH CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ISOTEKINDO INTERTAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
SEASIGHT ESR Test Pipette (3.8% Sodium Citrate)
Analysis ID: AKL 20206420018

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ISOTEKINDO INTERTAMA

AR Address

Jl. Raya Kebayoran Lama No. 309 C RW 01

Registration Date

Sep 19, 2024

Expiry Date

Mar 20, 2028

Product Type

Manual Hematology Equipment

Erythrocyte sedimentation rate test

Invitro Diagnostics

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